首页> 外文期刊>Chemistry of heterocyclic compounds >Syntheses Based on 4-Chloro-1-[3,5-di(trifluoromethyl)phenyl]-, 4-Chloro-1-(2,4-difluorophenyl)-5-formyl-3-methyl-6,7-dihydroindazoles, and 4-Chloro-5-formyl-3-methyl-1-(2-pyridyl)-6,7-dihydroindazoles
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Syntheses Based on 4-Chloro-1-[3,5-di(trifluoromethyl)phenyl]-, 4-Chloro-1-(2,4-difluorophenyl)-5-formyl-3-methyl-6,7-dihydroindazoles, and 4-Chloro-5-formyl-3-methyl-1-(2-pyridyl)-6,7-dihydroindazoles

机译:基于4-氯-1- [3,5-二(三氟甲基)苯基]-,4-氯-1-(2,4-二氟苯基)-5-甲酰基-3-甲基-6,7-二氢吲唑的合成,和4-氯-5-甲酰基-3-甲基-1-(2-吡啶基)-6,7-二氢吲唑

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摘要

Vilsmeier formylation of 1-[3,5-di(trifluoromethyl)phenyl]- and 1-(2,4-difluorophenyl)-3-methyl-4-oxo-4,5,6,7-tetrahydroindazoles gave the corresponding 1-aryl-4-chloro-5-formyl-3-methyl-6,7-dihydroindazoles. Reaction of the latter with amidines, o-phenylenediamine, hydrazine, or hydroxylamine gave a series of 1-aryl-3-methyl-6,6-dihydroindazoles annelated at positions 4 and 5. The reaction of 4-chloro-5-formyl-3-methyl-1-(2-pyridyl)-6,7-dihydroindazole with substituted anilines gave 5-arylaminomethylene-4-oxo- or 5-arylaminomethylene-4-arylimino-3-methyl-1-(2-pyridyl)-4,5,6,7-tetrahydroindazoles depending on the molar ratio of reagents and the nucleophilicity of the amines.
机译:1- [3,5-二(三氟甲基)苯基]-和1-(2,4-二氟苯基)-3-甲基-4-氧代-4,5,6,7-四氢吲唑的Vilsmeier甲酰化反应得到相应的1-芳基-4-氯-5-甲酰基-3-甲基-6,7-二氢吲唑。后者与am,邻苯二胺,肼或羟胺反应,得到一系列在位置4和5退火的1-芳基-3-甲基-6,6-二氢吲唑。4-氯-5-甲酰基- 3-甲基-1-(2-吡啶基)-6,7-二氢吲唑与取代的苯胺得到5-芳基氨基亚甲基-4-氧-或5-芳基氨基亚甲基-4-芳基-3-甲基-1-(2-吡啶基)- 4,5,6,7-四氢吲唑取决于试剂的摩尔比和胺的亲核性。

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